Loperamide Hydrochloride
- Product NDC
- 70518-0052
- 11-digit product format
- 705180052
- Labeler code
- 70518
- Product ID
- 70518-0052_984cc322-64ef-5341-e053-2a95a90a6580
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Loperamide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA073192
- Marketing category
- ANDA
- Marketing start
- 2016-12-12
- Marketing end
- 0000-00-00
- Substance
- LOPERAMIDE HYDROCHLORIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Opioid Agonist [EPC],Opioid Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record